Results 41 to 50 of about 1,400,939 (196)

SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome

, 2010
Purpose: The Mayer-Rokitansky-Kuster-Hauser syndrome is defined as congenital aplasia of mullerian ducts derived structures in females with a normal female chromosomal and gonadal sex. Most cases with Mayer-Rokitansky-Kuster-Hauser syndrome are sporadic,
L. Larizza, P. Colapietro, Monica Miozzo, B. Gentilin, Luigi Fedele, Laura Bernardini, L. Bernardini, Giada Frontino, G. Frontino, C.C.G. Gervasini, Cristina Gervasini, Patrizia Colapietro, Lidia Larizza, F. Lalatta, F. Motta, F. R. Grati, Silvia Tabano, B. Dallapiccola, Simona De Toffol, L. Fedele, Bruno Dallapiccola, Barbara Gentilin, S. Maitz, Francesca Romana Grati, Faustina Lalatta, S.M. Tabano, Francesca Motta, M.R. Miozzo, Silvia Maitz, S. De Toffol   +29 more
core   +1 more source

A rare form of Mayer-Rokitansky-Küster-Hauser syndrome: Case report and review of literature

Case Reports in Women's Health, 2019
Introduction: Primary amenorrhea is failure to reach menarche. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the second most common cause of primary amenorrhea, after gonadal dysgenesis.
Omran Al Dandan, Ali Hassan, Amna Alsaihati, Lujain Aljawad, Fathiya Almejhim   +4 more
doaj   +1 more source

Mayer-Rokitansky-Kuster-Hauser Syndrome: Diagnosis with MR Imaging [PDF]

Radiology, 2013
To evaluate the diverse magnetic resonance (MR) imaging findings of the pelvis in women with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome.This retrospective review had institutional review board approval with waiver of informed consent. Between 2001 and 2011, 215 female patients with MRKH syndrome attended clinics, and 66 underwent pelvic MR imaging (
Margaret Anne, Hall-Craggs, Cara Elizabeth, Williams, Sophie Helen, Pattison, Alex Paul, Kirkham, Sarah Margaret, Creighton   +4 more
openaire   +2 more sources

A case of Mayer Rokitansky Kuster Hauser syndrome

International Journal of Radiology and Diagnostic Imaging, 2019
Purpose & study object: We herewith present a case of unusual mullerian duct anomaly presenting with primary amenorrhea and some Past history suggestive of hymenotomy (details not available). Introduction: Mullerian duct anomaly is approximately 6.7% in general population. Incidence is higher in infertility 7.3% and recurrent miscarriages 16%.
Dr. Shikha Baid, Dr. Anil G Joshi
openaire   +2 more sources

Mayer-Rokitansky-Kuster-Hauser Syndrome [PDF]

Česká radiologie, 2020
Kara Bendle, Deborah Morse
  +4 more sources

Manejo laparoscópico de miomatosis uterina en pacientes con Síndrome de Rokitansky: Reporte de un caso y revisión de la literatura

Revista Colombiana de Obstetricia y Ginecología, 2013
Introducción: el síndrome de Mayer-Rokitansky-Küster-Hauser (SMRKH) es un espectro de anomalías de los conductos müllerianos caracterizado por la la ausencia congénita de útero y vagina en mujeres fenotípicamente normales, con cariotipo 46 XX, con un ...
Guillermo Páez-López, José Fernando De los Ríos-Posada, Adriana María Arango-Martínez, Juan David Castañeda-Roldán, Eduardo Serna-Agudelo, Ricardo Vásquez-Ruiz, Luis Alberto Almanza-Payares, Gustavo Adolfo Calle-Gómez   +7 more
doaj   +3 more sources

PSYCHOSOCIAL SUPPORT IN SELF-ACTUALIZING MAYER ROKITANSKY KUSTER HAUSER SYNDROME WOMEN

Nurse and Health, 2021
Background: Self-concept is an individual's mode to completely see his personality, dealing with intelligence, emotion, spirituality, physical form, or social form. It provides continuity, consistency, and completeness for an individual.
Gardha Rias Arsy, Retty Ratnawati
doaj   +1 more source

Lactation, Childrearing, and Gender Justice

Journal of Applied Philosophy, EarlyView.
ABSTRACT In this article, I discuss the significance of early infant feeding choices for the goal of gender justice. Focusing on human lactation practices, I identify Exclusive Gestational Nursing (EGN) as the norm in advanced industrial societies, which creates the expectation and permission for gestators, and only gestators, to nurse children, and ...
Jenny Brown
wiley   +1 more source

Differences in sex development among individuals with a female phenotype and an absent uterus: Diagnostic approach

Journal of International Medical Research
Objective To describe individuals with differences in sex development presenting with a female phenotype and an absent uterus and identify specific diagnostic characteristics that improve diagnostic accuracy and optimize patient care.
Ana Jibladze, Elene Asanidze, Alla Vash-Margita, Jenaro Kristesashvili   +3 more
doaj   +1 more source

Acute abdomen in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome

Vojnosanitetski pregled, 2008
Background. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a malformation of female genital tract (incidence 1 in 4000 female newborn children). It appears as a result of a disorder in the development of Millerian cannals. Etiology is unknown. Syndrome MRKH is the most frequent cause of primary amenorrhoea (90%).
Aleksandra Petric, Milan Stefanovic, Predrag Vukomanovic, Radomir Zivadinovic, Aleksandra Tubic, Zoran Janjic   +5 more
openaire   +3 more sources